Canonical Allele Identifier: CA1803237497
Gene: TMEM67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.93808908T= , CM000670.2:g.93808908T= GRCh38
NC_000008.10:g.94821136T= , CM000670.1:g.94821136T= GRCh37
NC_000008.9:g.94890312T= NCBI36
NG_009190.1:g.59065T= , LRG_688:g.59065T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323130.8:c.2508T= ENSP00000314488.4:p.Ser836=
ENST00000409623.8:c.2463T= ENSP00000386966.4:p.Ser821=
ENST00000452276.6:c.2391T= ENSP00000388671.2:p.Ser797=
ENST00000453906.6:c.1626T= ENSP00000403035.2:p.Ser542=
ENST00000518896.2:c.799T= ENSP00000507992.1:n.799T=
ENST00000520680.2:c.2631T= ENSP00000428785.2:p.Ser877=
ENST00000521517.6:c.2409T= ENSP00000430740.2:p.Ser803=
ENST00000681998.1:c.2329T= ENSP00000506773.1:n.2329T=
ENST00000682036.1:c.1749T= ENSP00000508390.1:p.Ser583=
ENST00000682577.1:c.2281T= ENSP00000506963.1:n.2281T=
ENST00000682624.1:c.*2082T= ENSP00000508343.1:n.*2082T=
ENST00000682700.1:c.2508T= ENSP00000507627.1:p.Ser836=
ENST00000682744.1:n.2046T=
ENST00000682804.1:n.2331T=
ENST00000682837.1:c.1997T= ENSP00000507920.1:n.1997T=
ENST00000682935.1:n.4558T=
ENST00000682984.1:c.2169T= ENSP00000507209.1:p.Ser723=
ENST00000683078.1:c.2263T= ENSP00000506796.1:n.2263T=
ENST00000683223.1:c.2240T= ENSP00000507685.1:n.2240T=
ENST00000683238.1:n.3732T=
ENST00000683249.1:n.4105T=
ENST00000683336.1:c.2329T= ENSP00000507695.1:n.2329T=
ENST00000683362.1:c.2169T= ENSP00000506985.1:p.Ser723=
ENST00000683850.1:n.2431T=
ENST00000683919.1:c.2438T= ENSP00000507617.1:n.2438T=
ENST00000683953.1:c.2419T= ENSP00000508375.1:n.2419T=
ENST00000684023.1:c.2485T= ENSP00000507461.1:n.2485T=
ENST00000684064.1:c.2199T= ENSP00000508192.1:p.Ser733=
ENST00000684089.1:n.4058T=
ENST00000684149.1:c.*1687T= ENSP00000507943.1:n.*1687T=
ENST00000684343.1:c.705T= ENSP00000507591.1:p.Ser235=
ENST00000684416.1:n.2467T=
ENST00000684540.1:c.2438T= ENSP00000507987.1:n.2438T=
ENST00000453321.8:c.2508T= MANE Select ENSP00000389998.3:p.Ser836=
ENST00000323130.7:c.2478T= ENSP00000314488.3:p.Ser826=
ENST00000409623.7:c.2265T= ENSP00000386966.3:p.Ser755=
ENST00000453321.7:c.2508T= ENSP00000389998.3:p.Ser836=
ENST00000474944.5:n.1646T=
ENST00000519845.5:n.1240T=
NM_001142301.1:c.2265T= , LRG_688t2:c.2265T= NP_001135773.1:p.Ser755=
NM_153704.5:c.2508T= , LRG_688t1:c.2508T= NP_714915.3:p.Ser836=
NR_024522.1:n.2579T=
XM_006716686.2:c.2205T= XP_006716749.1:p.Ser735=
XM_006716687.2:c.1908T= XP_006716750.1:p.Ser636=
XM_011517363.1:c.1626T= XP_011515665.1:p.Ser542=
XR_428387.1:n.2566T=
XR_928360.1:n.2566T=
XR_928361.1:n.2566T=
XR_928362.1:n.2566T=
XM_006716686.4:c.2205T= XP_006716749.1:p.Ser735=
XM_011517363.3:c.1626T= XP_011515665.1:p.Ser542=
XM_024447326.1:c.1854T= XP_024303094.1:p.Ser618=
XR_001745619.2:n.2549T=
XR_428387.2:n.2549T=
XR_928360.3:n.2549T=
XR_928362.3:n.2549T=
NM_153704.6:c.2508T= MANE Select NP_714915.3:p.Ser836=
NR_024522.2:n.2529T=